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Verified CAS / Academic Author2 Decoded Studies

Prof. SHI Haoyang

East China University of Science and Technology

Research Publications & English Decoded Briefs

Showing 2 publications
Chinese Journal of Environmental Engineering2026DOI: 10.12030/j.cjee.202508047

Multi-stage Activation of Fly Ash for Al(OH)3 Extraction: Process Optimization and Mechanistic Insights

Selective recovery of aluminum compounds from fly ash is a key route for its high-value utilization. This study developed a multi-stage activation process for extracting Al(OH)3 from fly ash, comprising mechanical activation, calcination activation, chemical separation, and carbonation precipitation. Fly ash was mixed with carbide slag and CaF2, then calcined; the resulting clinker was leached with Na2CO3 solution to extract Al. The CaO generated from high-temperature calcination of carbide slag facilitated the separation of Si and Al. After solid-liquid separation, CO2 was introduced into the Al-rich leachate to precipitate Al(OH)3. The process promoted the formation of Ca12Al14O32F2 and inert Ca2SiO4, achieving efficient Si-Al separation during calcination. Under optimal conditions (mechanical activation for 60 min, 4% CaF2, calcination at 1000°C for 2 h, leaching with 40 g/L Na2CO3), the Al extraction rate reached 91.8%, and the product purity was 98.9%. The alumina extraction residue exhibited porous and highly reactive characteristics, suitable for producing flame-retardant materials or high-value silicon-based products (e.g., white carbon black, molecular sieve adsorbents). The process offers a promising industrial route for fly ash valorization, with potential integration with cement production lines for synergistic CO2 capture and utilization.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-4036-4

Tuning interfacial water supply and electron transfer enables industrial-scale alkaline hydrogen evolution

Alkaline water electrolysis is a pivotal technology for large-scale green hydrogen production, yet its efficiency is constrained by sluggish hydrogen evolution reaction (HER) kinetics at industrial current densities. Here, we propose a synergistic dual-doping strategy to lower kinetic barriers for both Volmer and Heyrovsky steps. A robust amorphous NiCoV nanosheet electrode was synthesized via scalable one-step electrodeposition. In situ spectroscopic and kinetic characterizations reveal that hydrophilic V species optimize interfacial water by disrupting the hydrogen bond network, ensuring rapid supply of free water at the inner Helmholtz plane. Co dopants modulate electronic structure to facilitate electron transfer and optimize intermediate adsorption energetics. The NiCoV electrode requires an ultralow overpotential of 253 mV at -400 mA cm−2, surpassing most Pt-based catalysts, and maintains stability for over 200 h. Industrial validation in a scaled-up electrolyzer demonstrates a cell voltage of 1.89 V at 400 mA cm−2, achieving energy savings of 0.12 kWh m−3 H2 compared to commercial benchmarks. This translates to annual electricity savings of 1.33 × 10^6 kWh for a medium-scale demonstration project, highlighting immense potential for sustainable industrial applications.